Murphy B J, Laderoute K R, Short S M, Sutherland R M
Department of Cancer Biology, SRI International, Menlo Park, California 94025.
Br J Cancer. 1991 Jul;64(1):69-73. doi: 10.1038/bjc.1991.241.
Chronic hypoxia increases the expression of a set of stress proteins (oxygen regulated proteins or ORPs) which is implicated in the development of drug resistance and radiation sensitivity in tumour cells. Five major ORPs have been documented, and two, ORP 80 and ORP 100, are considered to be identical to the glucose regulated stress proteins GRP78 and GRP94, respectively. We report here that ORP 33 is a form of the heme catabolic enzyme, heme oxygenase, using evidence obtained from northern blotting, two-dimensional polyacrylamide gel electrophoresis and western analysis. Heme oxygenase is believed to be an important component of the cellular response to oxidative stress. The significance of heme oxygenase as a hypoxia-induced stress protein is discussed.
慢性缺氧会增加一组应激蛋白(氧调节蛋白或ORPs)的表达,这与肿瘤细胞耐药性和辐射敏感性的发展有关。已记录了五种主要的ORPs,其中两种,即ORP 80和ORP 100,分别被认为与葡萄糖调节应激蛋白GRP78和GRP94相同。我们在此报告,利用从Northern印迹、二维聚丙烯酰胺凝胶电泳和Western分析获得的证据,ORP 33是血红素分解代谢酶血红素加氧酶的一种形式。血红素加氧酶被认为是细胞对氧化应激反应的重要组成部分。本文讨论了血红素加氧酶作为缺氧诱导应激蛋白的意义。